Naumov G I, Naumova E S, Schnürer J
State Institute for Genetics and Selection of Industrial Microorganisms, Moscow, Russia.
Res Microbiol. 2001 Jul-Aug;152(6):551-62. doi: 10.1016/s0923-2508(01)01229-3.
We describe genetic, molecular and taxonomic characteristics of the yeast Hansenula anomala. Pulsed-field gel electrophoresis of chromosomal DNAs from 19 H. anomala strains and related species indicated that H. anomala had a clearly different karyotype. Chromosome length polymorphism of the H. anomala strains was independent of their geographic origin and source of isolation. The strains were classified into four groups of similar karyotypes and one strain showed a unique profile. The sizes of chromosomes ranged from 850 to 3500 kb in different strains. The haploid chromosome number of H. anomala is at least nine. We have found RAPD primers discriminating at both the species and strain levels. All the primers tested except the M13 core sequence generated unique patterns with most strains. The results indicate the usefulness of PCR analysis with primer M13 for identification of the H. anomala species. Screening of the CBS (Utrecht) collection strains of H. anomala showed that they are rather difficult objects for genetic hybridization analysis. The strains have low fertility, viz. very poor sporulation, low mating type activities and, as a rule, nonviable ascospores. The majority of the hybrids obtained are polyploid, probably tetraploid, as judged by the segregation of control auxotrophic markers. Nevertheless, some monosporic cultures of the strains studied, including the biocontrol yeast J121, formed diploid hybrids with regular meiotic segregation of control auxotrophic markers. As a rule, H. anomala isolates are homothallic, showing delayed self-diploidization. Rare stable heterothallic strains of H. anomala also occur.
我们描述了异常汉逊酵母的遗传、分子和分类学特征。对19株异常汉逊酵母菌株及相关物种的染色体DNA进行脉冲场凝胶电泳分析表明,异常汉逊酵母具有明显不同的核型。异常汉逊酵母菌株的染色体长度多态性与其地理起源和分离来源无关。这些菌株被分为四组核型相似的群体,还有一株显示出独特的图谱。不同菌株的染色体大小在850至3500 kb之间。异常汉逊酵母的单倍体染色体数至少为9条。我们发现随机扩增多态性DNA(RAPD)引物在物种和菌株水平上都具有鉴别能力。除M13核心序列外,所有测试引物在大多数菌株中都产生了独特的图谱。结果表明,用引物M13进行PCR分析对鉴别异常汉逊酵母物种是有用的。对异常汉逊酵母CBS(乌得勒支)保藏菌株的筛选表明,它们是遗传杂交分析相当困难的对象。这些菌株育性低,即产孢很差、交配型活性低,并且通常子囊孢子无活力。根据对照营养缺陷型标记的分离情况判断,获得的大多数杂种是多倍体,可能是四倍体。然而,所研究菌株的一些单孢培养物,包括生防酵母J121,形成了具有对照营养缺陷型标记常规减数分裂分离的二倍体杂种。通常,异常汉逊酵母分离株是同宗配合的,表现出延迟的自体二倍体化。也存在罕见的稳定异宗配合的异常汉逊酵母菌株。